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Structure of 875071-97-9
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This spirocyclic indole derivative features a brominated cyclopropane ring fused to an indole core, enabling direct functionalization in C–H activation and cross-coupling reactions. The electron-deficient cyclopropane enhances reactivity in transition-metal catalyzed processes, while the ketone group provides a handle for further derivatization. Bench-stable and moisture-tolerant, it streamlines access to complex heterocycles in synthetic and medicinal chemistry.
5'-Bromo-1',2'-dihydrospiro[cyclopropane-1,3'-indole]-2'-one serves as a versatile building block for the construction of spirocyclic indole scaffolds prevalent in bioactive molecules. The bromine substituent enables palladium-catalyzed cross-coupling reactions, while the cyclopropane-indole fusion provides structural rigidity and enhanced metabolic stability. Its bench-stable nature and compatibility with standard synthetic protocols facilitate efficient access to complex heterocyclic architectures in medicinal chemistry and process development workflows.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362-P405-P501
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Lot numbers can be found on the outside label of a product: